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Research Article: Molecular Detection of Hemoglobin O-Arab in the Sudanese Population

Date Published: 2023-08-03

Introduction:
Sickle cell disease is an inherited chronic hemolytic anemia whose clinical manifestations arise from the tendency of the hemoglobin (HbS or sickle hemoglobin) to polymerize and deform red blood cells into the characteristic sickle shape.

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